A case of long QT syndrome having compound mutations of KCNH2 and SCN5A.
Ito S, Taketani T, Sugamori T, Okada T, Sato H, Adachi T, Takeda M, Kodani N, Takahashi N, Endo A, Yoshitomi H, Tanabe K, Shimizu W.
Ito S, et al. Among authors: takahashi n.
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J Cardiol Cases. 2012.
PMID: 30533098
Free PMC article.